Hydrochloric Acid → 2-[(1-tert-Butyl)-1H-tetrazol-5-yl]phenylboronic acid

HRID 1440454Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1440454
[C:1]([N:5]1[C:9]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2Br)=[N:8][N:7]=[N:6]1)([CH3:4])([CH3:3])[CH3:2].[B:17](OC(C)C)([O:22]C(C)C)[O:18]C(C)C.Cl>C1COCC1.BrCCBr>[C:1]([N:5]1[C:9]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[B:17]([OH:22])[OH:18])=[N:8][N:7]=[N:6]1)([CH3:4])([CH3:3])[CH3:2]

Komponenten

6

Versuchsvorschrift

To dry Mg turnings (76 mg, 3.13 mmol) in THF (1 mL) was added a solution of 1-tert-butyl-5-(2-bromophenyl)-1H-tetrazole (733 mg, 2.61 mmol) in THF (1.5 mL), 1,2-Dibromoethane (20 mL) was added and the mixture was warmed slightly with a heat gun. After 5 min, triisopropyl borate (564 mg, 3.00 mmol) was added and the mixture was stirred at room temperature for 23 h. Ice and 0.5 N HCl (7 mL) were added and the mixture was stirred for 5 min. The mixture was extracted with ether, and the combined extracts were extracted with 1N KOH (10 mL). The aqueous extracts were filtered and acidified to pH 3 with 2N HCl. The precipitate was collected by filtration to give 306 mg (48%) of product as an off-white solid, mp 112°-115° C.

Aufarbeitung

  1. additionwas added
  2. temperaturethe mixture was warmed slightly with a heat gun
  3. stirringthe mixture was stirred for 5 min
  4. extractionThe mixture was extracted with ether
  5. extractionthe combined extracts were extracted with 1N KOH (10 mL)
  6. filtrationThe aqueous extracts were filtered
  7. filtrationThe precipitate was collected by filtration

Quellen und Nachweise

ORD-Eintrag
ord-9f6d11ca37e94e23a068d368b7e5b3cc
Quelldatensatz
uspto-grants-1996_03
Patentnummer
US05498776

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